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Distinct structural and dynamic components of portal hypertension in different animal models and human liver disease etiologies
Hepatology ( IF 13.5 ) Pub Date : 2021-10-30 , DOI: 10.1002/hep.32220
Philipp Königshofer 1, 2, 3, 4, 5 , Benedikt Silvester Hofer 1, 2, 3, 4 , Ksenia Brusilovskaya 1, 2, 3, 4, 5 , Benedikt Simbrunner 1, 2, 3, 4, 5, 6 , Oleksandr Petrenko 1, 2, 3, 4, 5 , Katharina Wöran 7 , Merima Herac 7 , Judith Stift 7 , Katharina Lampichler 8 , Gerald Timelthaler 9 , David Bauer 1, 2, 6 , Lukas Hartl 1, 2, 6 , Bernhard Robl 10 , Maria Sibila 10 , Bruno K Podesser 11 , Georg Oberhuber 12 , Philipp Schwabl 1, 2, 3, 4, 5, 6 , Mattias Mandorfer 1, 6 , Michael Trauner 1 , Thomas Reiberger 1, 2, 3, 4, 5, 6
Affiliation  

Liver fibrosis is the static and main (70%-80%) component of portal hypertension (PH). We investigated dynamic components of PH by a three-dimensional analysis based on correlation of hepatic collagen proportionate area (CPA) with portal pressure (PP) in animals or HVPG in patients.

中文翻译:

不同动物模型和人类肝病病因中门静脉高压的不同结构和动态成分

肝纤维化是门静脉高压症 (PH) 的静态和主要 (70%-80%) 组成部分。我们通过基于肝胶原比例面积 (CPA) 与动物门静脉压力 (PP) 或患者 HVPG 相关性的三维分析来研究 PH 的动态成分。
更新日期:2021-10-30
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